Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025G04Rik |
T |
A |
1: 151,769,150 (GRCm39) |
T121S |
possibly damaging |
Het |
4930503E14Rik |
T |
C |
14: 44,406,641 (GRCm39) |
E136G |
probably damaging |
Het |
Adgrg4 |
A |
G |
X: 56,005,320 (GRCm39) |
N2527S |
probably damaging |
Het |
Ak1 |
G |
A |
2: 32,519,593 (GRCm39) |
S7N |
probably benign |
Het |
Aktip |
A |
C |
8: 91,852,466 (GRCm39) |
I230R |
possibly damaging |
Het |
Alms1 |
A |
G |
6: 85,598,271 (GRCm39) |
I1032M |
probably damaging |
Het |
Asb4 |
T |
A |
6: 5,423,651 (GRCm39) |
V266E |
probably damaging |
Het |
Bace1 |
G |
A |
9: 45,765,962 (GRCm39) |
V130M |
probably damaging |
Het |
Bglap |
A |
T |
3: 88,291,744 (GRCm39) |
|
probably benign |
Het |
Brpf3 |
T |
C |
17: 29,040,233 (GRCm39) |
S885P |
probably benign |
Het |
Col9a2 |
T |
A |
4: 120,909,586 (GRCm39) |
I415N |
probably damaging |
Het |
Cybc1 |
A |
T |
11: 121,115,528 (GRCm39) |
|
probably null |
Het |
Dnajc7 |
T |
C |
11: 100,492,607 (GRCm39) |
Y38C |
probably benign |
Het |
Dync2i2 |
A |
G |
2: 29,922,820 (GRCm39) |
L309P |
probably benign |
Het |
Enam |
A |
G |
5: 88,651,236 (GRCm39) |
Y840C |
probably damaging |
Het |
Etnppl |
T |
A |
3: 130,425,442 (GRCm39) |
C416S |
probably damaging |
Het |
Fgf20 |
A |
T |
8: 40,732,896 (GRCm39) |
S181T |
probably benign |
Het |
Fut8 |
T |
A |
12: 77,510,835 (GRCm39) |
Y421N |
probably damaging |
Het |
Gcn1 |
T |
G |
5: 115,737,147 (GRCm39) |
L1295R |
probably damaging |
Het |
Gm11437 |
A |
G |
11: 84,055,337 (GRCm39) |
V93A |
probably benign |
Het |
Gm9989 |
T |
C |
3: 81,829,549 (GRCm39) |
|
noncoding transcript |
Het |
Gsdmc4 |
A |
T |
15: 63,765,736 (GRCm39) |
|
probably null |
Het |
Gvin3 |
T |
A |
7: 106,198,772 (GRCm39) |
|
noncoding transcript |
Het |
Ighv10-1 |
A |
T |
12: 114,442,643 (GRCm39) |
M114K |
probably benign |
Het |
Il22b |
T |
C |
10: 118,126,115 (GRCm39) |
I161V |
probably damaging |
Het |
Itfg2 |
T |
A |
6: 128,387,413 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
G |
A |
3: 86,995,774 (GRCm39) |
Q387* |
probably null |
Het |
Klk1 |
C |
T |
7: 43,876,968 (GRCm39) |
R24* |
probably null |
Het |
Klra7 |
T |
C |
6: 130,208,612 (GRCm39) |
|
probably null |
Het |
Ltn1 |
T |
C |
16: 87,213,118 (GRCm39) |
Y481C |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mrps2 |
A |
G |
2: 28,359,782 (GRCm39) |
N213S |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,569,869 (GRCm39) |
I310F |
possibly damaging |
Het |
Ntrk3 |
T |
A |
7: 78,167,185 (GRCm39) |
Y102F |
probably damaging |
Het |
Or8k24 |
A |
T |
2: 86,216,431 (GRCm39) |
C110* |
probably null |
Het |
Otof |
C |
T |
5: 30,556,635 (GRCm39) |
G282D |
probably damaging |
Het |
Pcdhb2 |
A |
T |
18: 37,430,367 (GRCm39) |
|
probably null |
Het |
Pign |
A |
T |
1: 105,515,703 (GRCm39) |
|
probably null |
Het |
Plekha6 |
G |
A |
1: 133,222,416 (GRCm39) |
E1001K |
probably benign |
Het |
Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
Ppm1d |
A |
G |
11: 85,236,678 (GRCm39) |
T486A |
probably benign |
Het |
Pudp |
A |
G |
18: 50,701,329 (GRCm39) |
F135L |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,945 (GRCm39) |
N178T |
probably benign |
Het |
Rel |
A |
C |
11: 23,703,215 (GRCm39) |
|
probably null |
Het |
Sf3a1 |
T |
A |
11: 4,117,824 (GRCm39) |
F195L |
probably damaging |
Het |
Slc30a1 |
G |
C |
1: 191,639,401 (GRCm39) |
A95P |
probably damaging |
Het |
Slc47a2 |
T |
C |
11: 61,194,773 (GRCm39) |
T469A |
probably benign |
Het |
Slc4a10 |
A |
T |
2: 61,876,989 (GRCm39) |
M1L |
probably benign |
Het |
Slc8a1 |
T |
A |
17: 81,955,703 (GRCm39) |
D445V |
probably damaging |
Het |
Slc9a7 |
C |
T |
X: 20,071,793 (GRCm39) |
G113R |
probably damaging |
Het |
Spata31e5 |
T |
A |
1: 28,816,712 (GRCm39) |
D440V |
probably damaging |
Het |
Spic |
T |
C |
10: 88,511,545 (GRCm39) |
H237R |
possibly damaging |
Het |
Stk26 |
A |
G |
X: 49,977,910 (GRCm39) |
E317G |
probably benign |
Het |
Tex10 |
A |
T |
4: 48,459,355 (GRCm39) |
Y506* |
probably null |
Het |
Trhde |
T |
A |
10: 114,280,585 (GRCm39) |
R848* |
probably null |
Het |
Trpc5 |
T |
A |
X: 143,202,594 (GRCm39) |
R545* |
probably null |
Het |
Usp24 |
C |
T |
4: 106,216,286 (GRCm39) |
T379M |
possibly damaging |
Het |
Zfp783 |
A |
T |
6: 47,922,499 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Chd9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Chd9
|
APN |
8 |
91,752,020 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00547:Chd9
|
APN |
8 |
91,732,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00589:Chd9
|
APN |
8 |
91,742,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00640:Chd9
|
APN |
8 |
91,712,760 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00663:Chd9
|
APN |
8 |
91,710,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00852:Chd9
|
APN |
8 |
91,699,835 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00908:Chd9
|
APN |
8 |
91,723,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00911:Chd9
|
APN |
8 |
91,778,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Chd9
|
APN |
8 |
91,768,744 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01668:Chd9
|
APN |
8 |
91,753,404 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01873:Chd9
|
APN |
8 |
91,660,395 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01969:Chd9
|
APN |
8 |
91,760,138 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02105:Chd9
|
APN |
8 |
91,659,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Chd9
|
APN |
8 |
91,683,122 (GRCm39) |
nonsense |
probably null |
|
IGL02164:Chd9
|
APN |
8 |
91,659,849 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02725:Chd9
|
APN |
8 |
91,778,312 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02755:Chd9
|
APN |
8 |
91,760,210 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02892:Chd9
|
APN |
8 |
91,703,543 (GRCm39) |
splice site |
probably benign |
|
IGL02897:Chd9
|
APN |
8 |
91,660,496 (GRCm39) |
splice site |
probably benign |
|
IGL03005:Chd9
|
APN |
8 |
91,738,075 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03062:Chd9
|
APN |
8 |
91,741,895 (GRCm39) |
splice site |
probably benign |
|
IGL03140:Chd9
|
APN |
8 |
91,768,856 (GRCm39) |
missense |
possibly damaging |
0.91 |
hovel
|
UTSW |
8 |
91,741,832 (GRCm39) |
missense |
probably benign |
0.19 |
shack
|
UTSW |
8 |
91,659,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Chd9
|
UTSW |
8 |
91,660,165 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0157:Chd9
|
UTSW |
8 |
91,735,464 (GRCm39) |
splice site |
probably null |
|
R0238:Chd9
|
UTSW |
8 |
91,659,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Chd9
|
UTSW |
8 |
91,659,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0432:Chd9
|
UTSW |
8 |
91,721,078 (GRCm39) |
splice site |
probably benign |
|
R0454:Chd9
|
UTSW |
8 |
91,699,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0573:Chd9
|
UTSW |
8 |
91,725,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Chd9
|
UTSW |
8 |
91,721,191 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0604:Chd9
|
UTSW |
8 |
91,763,170 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0662:Chd9
|
UTSW |
8 |
91,704,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R0825:Chd9
|
UTSW |
8 |
91,777,825 (GRCm39) |
missense |
probably benign |
0.06 |
R0945:Chd9
|
UTSW |
8 |
91,659,630 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0964:Chd9
|
UTSW |
8 |
91,741,832 (GRCm39) |
missense |
probably benign |
0.19 |
R0967:Chd9
|
UTSW |
8 |
91,716,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Chd9
|
UTSW |
8 |
91,659,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R1066:Chd9
|
UTSW |
8 |
91,712,764 (GRCm39) |
nonsense |
probably null |
|
R1244:Chd9
|
UTSW |
8 |
91,749,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1505:Chd9
|
UTSW |
8 |
91,733,123 (GRCm39) |
splice site |
probably null |
|
R1570:Chd9
|
UTSW |
8 |
91,763,170 (GRCm39) |
missense |
probably benign |
0.03 |
R1591:Chd9
|
UTSW |
8 |
91,710,166 (GRCm39) |
missense |
probably damaging |
0.97 |
R1624:Chd9
|
UTSW |
8 |
91,725,163 (GRCm39) |
missense |
probably benign |
0.17 |
R1626:Chd9
|
UTSW |
8 |
91,721,224 (GRCm39) |
missense |
probably benign |
0.00 |
R1632:Chd9
|
UTSW |
8 |
91,683,335 (GRCm39) |
nonsense |
probably null |
|
R1649:Chd9
|
UTSW |
8 |
91,659,229 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1664:Chd9
|
UTSW |
8 |
91,749,418 (GRCm39) |
splice site |
probably null |
|
R1668:Chd9
|
UTSW |
8 |
91,767,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R1681:Chd9
|
UTSW |
8 |
91,699,763 (GRCm39) |
missense |
probably damaging |
0.98 |
R1695:Chd9
|
UTSW |
8 |
91,728,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Chd9
|
UTSW |
8 |
91,760,853 (GRCm39) |
utr 3 prime |
probably benign |
|
R1746:Chd9
|
UTSW |
8 |
91,737,326 (GRCm39) |
missense |
probably benign |
0.01 |
R1843:Chd9
|
UTSW |
8 |
91,737,422 (GRCm39) |
missense |
probably benign |
0.19 |
R1844:Chd9
|
UTSW |
8 |
91,683,323 (GRCm39) |
nonsense |
probably null |
|
R1941:Chd9
|
UTSW |
8 |
91,703,697 (GRCm39) |
critical splice donor site |
probably null |
|
R2022:Chd9
|
UTSW |
8 |
91,761,682 (GRCm39) |
missense |
probably benign |
0.17 |
R2027:Chd9
|
UTSW |
8 |
91,634,619 (GRCm39) |
unclassified |
probably benign |
|
R2098:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2099:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2100:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2101:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2224:Chd9
|
UTSW |
8 |
91,737,913 (GRCm39) |
missense |
probably benign |
0.04 |
R2276:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2278:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2316:Chd9
|
UTSW |
8 |
91,777,756 (GRCm39) |
missense |
probably damaging |
0.99 |
R2507:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2508:Chd9
|
UTSW |
8 |
91,760,615 (GRCm39) |
missense |
probably benign |
0.01 |
R2988:Chd9
|
UTSW |
8 |
91,757,088 (GRCm39) |
splice site |
probably null |
|
R3418:Chd9
|
UTSW |
8 |
91,763,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R3817:Chd9
|
UTSW |
8 |
91,710,893 (GRCm39) |
splice site |
probably benign |
|
R3923:Chd9
|
UTSW |
8 |
91,660,147 (GRCm39) |
missense |
probably benign |
0.16 |
R4001:Chd9
|
UTSW |
8 |
91,683,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4003:Chd9
|
UTSW |
8 |
91,683,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4006:Chd9
|
UTSW |
8 |
91,660,188 (GRCm39) |
missense |
probably benign |
0.12 |
R4013:Chd9
|
UTSW |
8 |
91,699,797 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4108:Chd9
|
UTSW |
8 |
91,737,304 (GRCm39) |
missense |
probably benign |
0.04 |
R4125:Chd9
|
UTSW |
8 |
91,777,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R4126:Chd9
|
UTSW |
8 |
91,777,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R4452:Chd9
|
UTSW |
8 |
91,704,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R4463:Chd9
|
UTSW |
8 |
91,705,627 (GRCm39) |
missense |
probably benign |
0.01 |
R4478:Chd9
|
UTSW |
8 |
91,760,659 (GRCm39) |
utr 3 prime |
probably benign |
|
R4587:Chd9
|
UTSW |
8 |
91,763,134 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4628:Chd9
|
UTSW |
8 |
91,710,091 (GRCm39) |
missense |
probably benign |
0.05 |
R4667:Chd9
|
UTSW |
8 |
91,760,428 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4908:Chd9
|
UTSW |
8 |
91,741,877 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4912:Chd9
|
UTSW |
8 |
91,760,858 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4977:Chd9
|
UTSW |
8 |
91,760,336 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5016:Chd9
|
UTSW |
8 |
91,733,254 (GRCm39) |
nonsense |
probably null |
|
R5083:Chd9
|
UTSW |
8 |
91,711,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Chd9
|
UTSW |
8 |
91,704,147 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5090:Chd9
|
UTSW |
8 |
91,753,462 (GRCm39) |
nonsense |
probably null |
|
R5307:Chd9
|
UTSW |
8 |
91,723,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Chd9
|
UTSW |
8 |
91,778,132 (GRCm39) |
missense |
probably benign |
0.09 |
R5559:Chd9
|
UTSW |
8 |
91,742,553 (GRCm39) |
critical splice donor site |
probably null |
|
R5638:Chd9
|
UTSW |
8 |
91,738,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5640:Chd9
|
UTSW |
8 |
91,763,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Chd9
|
UTSW |
8 |
91,728,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R5827:Chd9
|
UTSW |
8 |
91,716,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Chd9
|
UTSW |
8 |
91,723,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5875:Chd9
|
UTSW |
8 |
91,778,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R6002:Chd9
|
UTSW |
8 |
91,705,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Chd9
|
UTSW |
8 |
91,761,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6185:Chd9
|
UTSW |
8 |
91,775,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Chd9
|
UTSW |
8 |
91,659,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Chd9
|
UTSW |
8 |
91,659,550 (GRCm39) |
missense |
probably benign |
0.05 |
R6305:Chd9
|
UTSW |
8 |
91,757,174 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6348:Chd9
|
UTSW |
8 |
91,737,903 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6438:Chd9
|
UTSW |
8 |
91,725,149 (GRCm39) |
missense |
probably benign |
0.02 |
R6470:Chd9
|
UTSW |
8 |
91,659,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Chd9
|
UTSW |
8 |
91,778,182 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6902:Chd9
|
UTSW |
8 |
91,769,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Chd9
|
UTSW |
8 |
91,683,044 (GRCm39) |
missense |
probably benign |
0.02 |
R6929:Chd9
|
UTSW |
8 |
91,769,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Chd9
|
UTSW |
8 |
91,705,542 (GRCm39) |
missense |
probably benign |
0.34 |
R7043:Chd9
|
UTSW |
8 |
91,760,843 (GRCm39) |
utr 3 prime |
probably benign |
|
R7094:Chd9
|
UTSW |
8 |
91,716,189 (GRCm39) |
missense |
unknown |
|
R7126:Chd9
|
UTSW |
8 |
91,741,853 (GRCm39) |
missense |
unknown |
|
R7182:Chd9
|
UTSW |
8 |
91,733,250 (GRCm39) |
missense |
unknown |
|
R7219:Chd9
|
UTSW |
8 |
91,728,394 (GRCm39) |
missense |
unknown |
|
R7260:Chd9
|
UTSW |
8 |
91,721,171 (GRCm39) |
missense |
unknown |
|
R7293:Chd9
|
UTSW |
8 |
91,760,707 (GRCm39) |
missense |
unknown |
|
R7303:Chd9
|
UTSW |
8 |
91,778,532 (GRCm39) |
missense |
unknown |
|
R7358:Chd9
|
UTSW |
8 |
91,760,846 (GRCm39) |
missense |
unknown |
|
R7358:Chd9
|
UTSW |
8 |
91,710,115 (GRCm39) |
missense |
unknown |
|
R7451:Chd9
|
UTSW |
8 |
91,760,446 (GRCm39) |
missense |
probably benign |
0.27 |
R7451:Chd9
|
UTSW |
8 |
91,760,418 (GRCm39) |
frame shift |
probably null |
|
R7456:Chd9
|
UTSW |
8 |
91,659,153 (GRCm39) |
nonsense |
probably null |
|
R7481:Chd9
|
UTSW |
8 |
91,683,066 (GRCm39) |
missense |
unknown |
|
R7532:Chd9
|
UTSW |
8 |
91,721,193 (GRCm39) |
missense |
unknown |
|
R7570:Chd9
|
UTSW |
8 |
91,721,208 (GRCm39) |
missense |
unknown |
|
R7611:Chd9
|
UTSW |
8 |
91,763,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Chd9
|
UTSW |
8 |
91,778,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R7723:Chd9
|
UTSW |
8 |
91,741,837 (GRCm39) |
missense |
unknown |
|
R7739:Chd9
|
UTSW |
8 |
91,761,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Chd9
|
UTSW |
8 |
91,704,178 (GRCm39) |
critical splice donor site |
probably null |
|
R7916:Chd9
|
UTSW |
8 |
91,761,684 (GRCm39) |
nonsense |
probably null |
|
R7921:Chd9
|
UTSW |
8 |
91,768,909 (GRCm39) |
critical splice donor site |
probably null |
|
R7957:Chd9
|
UTSW |
8 |
91,778,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R7972:Chd9
|
UTSW |
8 |
91,732,395 (GRCm39) |
missense |
unknown |
|
R8108:Chd9
|
UTSW |
8 |
91,659,852 (GRCm39) |
missense |
unknown |
|
R8115:Chd9
|
UTSW |
8 |
91,762,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R8165:Chd9
|
UTSW |
8 |
91,767,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Chd9
|
UTSW |
8 |
91,752,015 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8186:Chd9
|
UTSW |
8 |
91,725,233 (GRCm39) |
missense |
unknown |
|
R8208:Chd9
|
UTSW |
8 |
91,763,891 (GRCm39) |
splice site |
probably null |
|
R8256:Chd9
|
UTSW |
8 |
91,660,129 (GRCm39) |
missense |
unknown |
|
R8281:Chd9
|
UTSW |
8 |
91,763,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Chd9
|
UTSW |
8 |
91,723,472 (GRCm39) |
missense |
unknown |
|
R8836:Chd9
|
UTSW |
8 |
91,767,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R8892:Chd9
|
UTSW |
8 |
91,660,468 (GRCm39) |
missense |
unknown |
|
R8985:Chd9
|
UTSW |
8 |
91,721,101 (GRCm39) |
missense |
unknown |
|
R9029:Chd9
|
UTSW |
8 |
91,683,198 (GRCm39) |
missense |
unknown |
|
R9030:Chd9
|
UTSW |
8 |
91,683,198 (GRCm39) |
missense |
unknown |
|
R9038:Chd9
|
UTSW |
8 |
91,716,233 (GRCm39) |
missense |
unknown |
|
R9081:Chd9
|
UTSW |
8 |
91,704,144 (GRCm39) |
nonsense |
probably null |
|
R9134:Chd9
|
UTSW |
8 |
91,659,754 (GRCm39) |
missense |
unknown |
|
R9205:Chd9
|
UTSW |
8 |
91,757,270 (GRCm39) |
missense |
probably benign |
0.01 |
R9309:Chd9
|
UTSW |
8 |
91,733,319 (GRCm39) |
missense |
unknown |
|
R9375:Chd9
|
UTSW |
8 |
91,725,335 (GRCm39) |
critical splice donor site |
probably null |
|
R9449:Chd9
|
UTSW |
8 |
91,659,174 (GRCm39) |
missense |
unknown |
|
R9547:Chd9
|
UTSW |
8 |
91,683,186 (GRCm39) |
missense |
unknown |
|
R9573:Chd9
|
UTSW |
8 |
91,704,302 (GRCm39) |
missense |
unknown |
|
R9576:Chd9
|
UTSW |
8 |
91,659,294 (GRCm39) |
missense |
unknown |
|
R9601:Chd9
|
UTSW |
8 |
91,732,360 (GRCm39) |
nonsense |
probably null |
|
R9613:Chd9
|
UTSW |
8 |
91,683,150 (GRCm39) |
nonsense |
probably null |
|
R9639:Chd9
|
UTSW |
8 |
91,760,840 (GRCm39) |
missense |
probably null |
|
R9718:Chd9
|
UTSW |
8 |
91,712,801 (GRCm39) |
missense |
unknown |
|
R9746:Chd9
|
UTSW |
8 |
91,738,063 (GRCm39) |
missense |
unknown |
|
R9762:Chd9
|
UTSW |
8 |
91,712,741 (GRCm39) |
missense |
unknown |
|
R9764:Chd9
|
UTSW |
8 |
91,721,220 (GRCm39) |
missense |
unknown |
|
R9790:Chd9
|
UTSW |
8 |
91,760,417 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9791:Chd9
|
UTSW |
8 |
91,760,417 (GRCm39) |
missense |
possibly damaging |
0.82 |
RF007:Chd9
|
UTSW |
8 |
91,760,578 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0065:Chd9
|
UTSW |
8 |
91,763,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|